Interneurone

Résumé

Un interneurone est un neurone multipolaire qui établit de multiples connexions entre un réseau afférent et un réseau efférent. Comme les motoneurones, leur corps cellulaire est toujours situé dans le système nerveux central (SNC). La majorité des interneurones sont inhibiteurs et sécrètent un neurotransmetteur caractéristique, le GABA. Interneurones centraux En comparaison du système nerveux périphérique (SNP), les neurones du système nerveux central peuvent être considérés comme des interneurones. Néanmoins, dans le système nerveux central, le terme interneurone désigne des petits neurones qui ont des prolongements (axoniques et dendritiques) à faible distance (au contraire des larges neurones pyramidaux qui assurent des connexions à longue distance entre différentes aires cérébrales). Les interneurones du système nerveux central sont principalement inhibiteurs et sécrètent du GABA ou de la glycine. Néanmoins, il existe des interneurones excitateurs qui sécrètent du glu

Source officielle

À propos de ce résultat

Cette page est générée automatiquement et peut contenir des informations qui ne sont pas correctes, complètes, à jour ou pertinentes par rapport à votre recherche. Il en va de même pour toutes les autres pages de ce site. Veillez à vérifier les informations auprès des sources officielles de l'EPFL.

Publications associées

Chargement

Personnes associées

Chargement

Unités associées

Chargement

Concepts associés

Chargement

Cours associés

Chargement

Séances de cours associées

Chargement

A subpopulation of cortical VIP-expressing interneurons with highly dynamic spines

Jérôme Blanc, Christina Georgiou, Graham Knott, Kok Sin Lee

Structural synaptic plasticity may underlie experience and learning-dependent changes in cortical circuits. In contrast to excitatory pyramidal neurons, insight into the structural plasticity of inhibitory neurons remains limited. Interneurons are divided into various subclasses, each with specialized functions in cortical circuits. Further knowledge of subclass-specific structural plasticity of interneurons is crucial to gaining a complete mechanistic understanding of their contribution to cortical plasticity overall. Here, we describe a subpopulation of superficial cortical multipolar interneurons expressing vasoactive intestinal peptide (VIP) with high spine densities on their dendrites located in layer (L) 1, and with the electrophysiological characteristics of bursting cells. Using longitudinal imaging in vivo, we found that the majority of the spines are highly dynamic, displaying lifetimes considerably shorter than that of spines on pyramidal neurons. Using correlative light and electron microscopy, we confirmed that these VIP spines are sites of excitatory synaptic contacts, and are morphologically distinct from other spines in L1. Advanced light and electron microscopy identify a subset of cortical multipolar vasoactive intestinal peptide interneurons with high spine dynamics and characteristics that are greatly different from pyramidal neurons.

NATURE PORTFOLIO2022

Chargement

Thalamic microcircuitry: neurons, synapses, and circuit motifs in receptive field structure and sensory processing

Jane Yi

Our perception of the world is first shaped by the thalamus, a structure composed of many nuclei in the center of our brains. Different nuclei hold different responsibilities - vision (dorsal lateral genicular nucleus; dLGN), audition (medial geniculate nucleus; MGN), somatosensation (ventro-basal nuclei; VB), though many properties across these sensory modalities appear to be universal. In this thesis, we completed a comprehensive characterization of the neurons, connections, and microcircuitries within the rodent VB thalamus. Our most prominent finding is the confirmation of the existence of local interneurons in the VB and the discovery of their profoundly active and diverse role in thalamic processes. Thus, we have observed that the fundamental excitatory and inhibitory neurons of dLGN and VB nuclei and their intrinsic circuit motifs are indistinguishable. Only a few notable differences are, however, present. (1), Principal excitatory neurons of the VB, the thalamocortical (TC) relays, have morphological types that appear to be distributed heteroge-neously throughout the VB whereas dLGN TC morphological types have regional preferences. (2), VB inhibitory local interneurons represent a smaller proportion of the total neuronal popula-tion compared to their dLGN counterparts. The similarities between these thalamic regions great-ly outnumber the differences. It then introduces new questions of how different vision and soma-tosensation of the physical world are when these senses are ultimately represented as binary sig-nals and are processed in similar manners in the thalamus. Following these questions may lead to new therapeutic solutions for retinally blind patients, tactile prostheses, or neurological disorders of sensory perception like schizophrenia.

EPFL2021

Chargement

, , ,

The binding of GABA (gamma-aminobutyric acid) to extrasynaptic GABA(A) receptors generates tonic inhibition that acts as a powerful modulator of cortical network activity. Despite GABA being present throughout the extracellular space of the brain, previous work has shown that GABA may differentially modulate the excitability of neuron subtypes according to variation in chloride gradient. Here, using biophysically detailed neuron models, we predict that tonic inhibition can differentially modulate the excitability of neuron subtypes according to variation in electrophysiological properties. Surprisingly, tonic inhibition increased the responsiveness (or gain) in models with features typical for somatostatin interneurons but decreased gain in models with features typical for parvalbumin interneurons. Patch-clamp recordings from cortical interneurons supported these predictions, and further in silico analysis was then performed to seek a putative mechanism underlying gain modulation. We found that gain modulation in models was dependent upon the magnitude of tonic current generated at depolarized membrane potential-a property associated with outward rectifying GABA(A) receptors. Furthermore, tonic inhibition produced two biophysical changes in models of relevance to neuronal excitability: 1) enhanced action potential repolarization via increased current flow into the dendritic compartment, and 2) reduced activation of voltage-dependent potassium channels. Finally, we show theoretically that reduced potassium channel activation selectively increases gain in models possessing action potential dynamics typical for somatostatin interneurons. Potassium channels in parvalbumin-type models deactivate rapidly and are unavailable for further modulation. These findings show that GABA can differentially modulate interneuron excitability and suggest a mechanism through which this occurs in silico via differences of intrinsic electrophysiological properties.

NATL ACAD SCIENCES2020

Chargement